Variant report

Variant rs9411268
Chromosome Location chr9:139600594-139600595
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139590600-139600800 Enhancers Primary hematopoietic stem cells blood
2 chr9:139593800-139605600 Weak transcription Liver Liver
3 chr9:139596200-139606200 Weak transcription Fetal Intestine Small intestine
4 chr9:139596400-139600800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr9:139596400-139606200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr9:139596400-139606200 Weak transcription Spleen Spleen
7 chr9:139598200-139600800 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr9:139598200-139601400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr9:139598200-139604000 Weak transcription Thymus Thymus
10 chr9:139598600-139600600 Enhancers Stomach Mucosa stomach
11 chr9:139599600-139600600 Enhancers Monocytes-CD14+_RO01746 blood
12 chr9:139599800-139600600 Enhancers K562 blood
13 chr9:139600000-139600600 Enhancers Rectal Smooth Muscle rectum
14 chr9:139600000-139602400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
15 chr9:139600200-139600800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr9:139600200-139600800 Bivalent Enhancer Placenta Placenta
17 chr9:139600200-139601400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
18 chr9:139600200-139606000 Weak transcription Adipose Nuclei Adipose
19 chr9:139600400-139600600 Bivalent Enhancer Primary monocytes fromperipheralblood blood

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